List of variants reported as benign for Fanconi anemia complementation group N

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.1676A>G (p.Gln559Arg)	rs152451	0.12980
NM_024675.4(PALB2):c.-47G>A	rs8053188	0.04991
NM_024675.4(PALB2):c.3300T>G (p.Thr1100=)	rs45516100	0.02529
NM_024675.4(PALB2):c.2014G>C (p.Glu672Gln)	rs45532440	0.02171
NM_024675.4(PALB2):c.629C>T (p.Pro210Leu)	rs57605939	0.02101
NM_024675.4(PALB2):c.2993G>A (p.Gly998Glu)	rs45551636	0.01717
NM_024675.4(PALB2):c.1010T>C (p.Leu337Ser)	rs45494092	0.01508
NM_024675.4(PALB2):c.2794G>A (p.Val932Met)	rs45624036	0.00449

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